US3279993A - Stabilized aqueous hemostatic preparation - Google Patents

Stabilized aqueous hemostatic preparation Download PDF

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Publication number
US3279993A
US3279993A US329526A US32952663A US3279993A US 3279993 A US3279993 A US 3279993A US 329526 A US329526 A US 329526A US 32952663 A US32952663 A US 32952663A US 3279993 A US3279993 A US 3279993A
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Prior art keywords
hemostatic
added
bisulfite
preparation
aqueous
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Expired - Lifetime
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US329526A
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English (en)
Inventor
Anraku Takao
Nagashima Renpei
Kobayashi Toshio
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Chugai Pharmaceutical Co Ltd
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Chugai Pharmaceutical Co Ltd
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    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00—Medicinal preparations characterised by special physical form
    • A61K9/0012—Galenical forms characterised by the site of application
    • A61K9/0019—Injectable compositions; Intramuscular, intravenous, arterial, subcutaneous administration; Compositions to be administered through the skin in an invasive manner
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K38/00—Medicinal preparations containing peptides
    • A61K38/16—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
    • A61K38/17—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
    • A61K38/36—Blood coagulation or fibrinolysis factors
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K14/00—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
    • C07K14/435—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
    • C07K14/745—Blood coagulation or fibrinolysis factors
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G69/00—Macromolecular compounds obtained by reactions forming a carboxylic amide link in the main chain of the macromolecule
    • C08G69/42—Polyamides containing atoms other than carbon, hydrogen, oxygen, and nitrogen
    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
    • C12N9/00—Enzymes; Proenzymes; Compositions thereof; Processes for preparing, activating, inhibiting, separating or purifying enzymes
    • C12N9/96—Stabilising an enzyme by forming an adduct or a composition; Forming enzyme conjugates
    • D—TEXTILES; PAPER
    • D01—NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
    • D01F—CHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
    • D01F8/00—Conjugated, i.e. bi- or multicomponent, artificial filaments or the like; Manufacture thereof
    • D01F8/04—Conjugated, i.e. bi- or multicomponent, artificial filaments or the like; Manufacture thereof from synthetic polymers
    • D01F8/12—Conjugated, i.e. bi- or multicomponent, artificial filaments or the like; Manufacture thereof from synthetic polymers with at least one polyamide as constituent

Definitions

  • a lipid-soluble antioxidant such as, for example, buty-l hydroxy anisole (BHA), nordihydroguaiaretic acid (NDGA), ethyl protocatechuate, a-tochopherol would be added to said fatty substances.
  • BHA buty-l hydroxy anisole
  • NDGA nordihydroguaiaretic acid
  • a-tochopherol a lipid-soluble antioxidant
  • the addition of said antioxidants to the aqueous dispersion ofthe phospholipid which we have proposed in Japanese patent, is made with difliculty because said antioxidants are lipid-soluble but watchinsoluble. Further most of said antioxidants are not preferable because of their liability to develop a reddish color upon standing under the light even in their sparingly dissolved aqueous solutions.
  • the present invention has been resulted from our studies for obtaining a stable aqueous dispersion of hemostatic phospholipid which can be kept for along period of time at room temperatures, without decreasing its hemostatic activity and coloring even in the presence of diiferent substances as amino acid being added at will and are able to administered both intravenously and intramuscularly.
  • a method for stabilizing phospholipid having hemostatic action in which one or more of water-soluble reducing agents having sulfur atom or atoms in its molecule is added as stabilizer to an aqueous dispersion of phospholipid.
  • Example of these reducing agents may be employed are sulfites, bisulfites, meta-bisulfites, thiosulfates, sulfoxylates, a-mono-thioglycerol.
  • the single figure consists of comparative graphs illustrating blood platelet activity with and without the incorporation of potassium metabisulfite for varying storage periods at different temperatures.
  • An aqueous dispersion of phospholipid having hemostatic action in this invention means such one as is obtained by dispersing phospholipid having hemostatic action represented by lipid th'romboplastin into water or water containing sodium chloride, amino acid, vitamin or the like.
  • the water soluble reducing agents having sulfur atom or atoms in the molecule which are employed in this invention as the stabilizers and their stabilizing effects will be concretely explained.
  • sodium sulfite Na SO sodium bisulfite (NaHSO potassium meta-bisulfite 3,279,993 Patented Oct. 18, 1966 "ice more of them are added to the aqueous dispersion of phospholipid having hemostatic action act to consume rongalite oxygen dissolved in water by being oxidized themselves and prevent the hemostatic substances from autooxidation and polymerization caused by oxygen.
  • an inert gas as such as nitrogen gas into water in the process when the hemostatic substance is dispersed in water.
  • oxygen contained in water may be replaced by the inert gas, whereupon the hemostatic substance may be prevented from being contacted with oxygen and the amount of the stabilizer to be employed may be saved.
  • a hemostatic agent as is free from decreasing of the activity and coloring and can be preserved for a long period of time at room temperature even in 'the presence of diiferen-t substance such as incorporated amino acid.
  • diiferen-t substance such as incorporated amino acid.
  • amina acid e-am-inocaproic acid, for example, which is commonly well known as an antifibrinolytic enzyme may be incorporated with the hemostatic substance.
  • the hemostatic preparation of this invention can be adjusted to pH 6.0-8.0 as will, so that it may be administered intravenously and intramuscularly.
  • N ddt' o a 1 ion B Addition of ascorbic acid ⁇ H1thert known method 0. Addition or potassium metabisulfite Method of the present D. Addition of a-mono-thioglycerol invention E. Addition of bisulfite F. Addition of rongalite The sample of freshly prepared C served as a control.
  • the hemostatic preparation stabilized by the method of this invention keeps extraordinarily high degree of relative whiteness and the stabilizers used present an excellent effect on prevention against coloration.
  • the blood platelet activity of the sample was measured by means of thromboplastin-forming tests described in Biggs and Douglas: J. Clin. Path. June 23, 1953, after standing for 3-20 days at various temperature conditions. As shown in the drawing, solid lines represent the percent to the original activity in the case of postassium meta-bisulfite being incorporated and broken lines not incorporated. In the former case excellent stabilizing effects of hemostatic action are observed upon standing at every temperature, whereas in the latter case the activities fall rapid-1y at every temperature.
  • Example 1 220 mg. of l-ipid-thromboplastin were added to 44 ml. of physiological solution containing 35.2 mg. of monionic surface active agent polyoxyethylene sonbitan monolaurate (Tween-20 produced by Atlas Powder Co.) while stirring and with introducing of nitrogen gas thereinto. After lipid-'thromboplastin, being finely dispersed, 44 mg. of potassium meta-bisulfite were added. The dispersion was then adjusted to pH 7.0 and filtered. Each cc. of thus obtained dispersion was sealed in brown arnpoule, each ampoule having been with nitrogen prior to sealing, and then sterilized at 100 C. for 40 minutes to obtain a product.
  • monionic surface active agent polyoxyethylene sonbitan monolaurate Teween-20 produced by Atlas Powder Co.
  • Example 2 24 mg. of nonionic surface active agent polyoxyethylene sorbitan monolaurate (Tween-20) and 2 g. of eaminocaproic acid were dissolved in distilled water to make 40 m1. of solution. To the solution, while stirring and introducing nitrogen gas therein, a solution of 500 mg. of lipid-thromboplastin in 6 cc. of ether were added and finely dispersed vol-atil-izing of ether, by heating to 50 C. on a water bath. After cooling to the room temperature 100 mg. of postassium meta-bisulfite were added to dissolve, the dispersion adjusted to pH 7.5 and filtered. Each 2 cc. of the dispersion thus obtained was sealed in brown ampoule each ampoule having been flushed with nitrogen prior to sealing and then sterilized.
  • Tween-20 nonionic surface active agent polyoxyethylene sorbitan monolaurate
  • Example 3 instead of 44 mg. of potassium meta-bisulfite 44 mg. of sodium bisulfite were added as in Example 1.
  • Example 4 instead of 100 mg. of postassium betabisulfite 100 mg. of sodium bisulfite were added as in Example 2.
  • Example 5 Instead of 44 mg. of postassium meta-bisulfite 44 mg. of sodium sulfite were added as in Example 1.
  • Example 6 Instead of mg. of postassium metabisulfite 100 mg. of sodium sulfite were added as in Example 2.
  • Example 7 Instead of 100 mg. of potassium meta-bisulfite 100 mg. of rongalite were added as in Example 2.
  • Example 8 instead of 100 mg. of postassium met-a-bisulfite 100 mg. of sodium thiosulfate were added as in Example 2.
  • the preparations above thus obtained do not suffer any undesirable changes such as coloration and the deterioration of hemostatic activity but are very stable and can be administered intravenously and intramuscularly.
  • An aqueous hemostatic preparation containing lipid- -thromboplastic which comprises a small amount of watersoluble reducing agent having at least one sulfur atom in its molecule and an aqueous dispersion of said lipidthromboplastin.
  • said reducing agent is selected from the group consisting of sodium sulfite, sodium bisulfite, potassium meta-bisulfite, sodium thiosulfate, rongalitie and a-rnonothioglycerol.

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  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Organic Chemistry (AREA)
  • Medicinal Chemistry (AREA)
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  • General Health & Medical Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Genetics & Genomics (AREA)
  • Epidemiology (AREA)
  • Wood Science & Technology (AREA)
  • Veterinary Medicine (AREA)
  • Gastroenterology & Hepatology (AREA)
  • Public Health (AREA)
  • Animal Behavior & Ethology (AREA)
  • Molecular Biology (AREA)
  • Proteomics, Peptides & Aminoacids (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Hematology (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Biochemistry (AREA)
  • General Chemical & Material Sciences (AREA)
  • Polymers & Plastics (AREA)
  • General Engineering & Computer Science (AREA)
  • Immunology (AREA)
  • Biomedical Technology (AREA)
  • Textile Engineering (AREA)
  • Biophysics (AREA)
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  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
US329526A 1962-12-20 1963-12-10 Stabilized aqueous hemostatic preparation Expired - Lifetime US3279993A (en)

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JP5611862 1962-12-20

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US (1) US3279993A (en:Method)
BE (1) BE641559A (en:Method)
CH (1) CH465139A (en:Method)
DE (1) DE1203909B (en:Method)
FR (1) FR3104M (en:Method)
GB (1) GB1018647A (en:Method)
NL (1) NL302091A (en:Method)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0043274A3 (en) * 1980-06-30 1982-01-20 T And R Chemicals, Inc. Antithrombotic treatment
EP0055702A1 (en) * 1980-06-30 1982-07-07 T And R Chemicals, Inc. Antithrombotic treatment
EP1462109A1 (en) * 2003-03-28 2004-09-29 D.M.G. Italia Srl Hemostatic, emollient and lubricating preparations containing pork fat extract (lard)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20060019868A1 (en) 2004-01-30 2006-01-26 Pendharkar Sanyog M Hemostatic compositions and devices
US7927626B2 (en) * 2003-08-07 2011-04-19 Ethicon, Inc. Process of making flowable hemostatic compositions and devices containing such compositions
US8440225B2 (en) 2003-08-07 2013-05-14 Ethicon, Inc. Process of making flowable hemostatic compositions and devices containing such compositions

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2047144A (en) * 1934-03-26 1936-07-07 Lilly Co Eli Stabilized epinephrine-type compound, and process of stabilizing it
US2719812A (en) * 1953-08-07 1955-10-04 Merck & Co Inc Stabilized aqueous solutions of streptomycin
US2970944A (en) * 1958-04-04 1961-02-07 Merck & Co Inc Parenteral solutions of steroid phosphates stabilized with creatinines

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2047144A (en) * 1934-03-26 1936-07-07 Lilly Co Eli Stabilized epinephrine-type compound, and process of stabilizing it
US2719812A (en) * 1953-08-07 1955-10-04 Merck & Co Inc Stabilized aqueous solutions of streptomycin
US2970944A (en) * 1958-04-04 1961-02-07 Merck & Co Inc Parenteral solutions of steroid phosphates stabilized with creatinines

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0043274A3 (en) * 1980-06-30 1982-01-20 T And R Chemicals, Inc. Antithrombotic treatment
EP0055702A1 (en) * 1980-06-30 1982-07-07 T And R Chemicals, Inc. Antithrombotic treatment
EP1462109A1 (en) * 2003-03-28 2004-09-29 D.M.G. Italia Srl Hemostatic, emollient and lubricating preparations containing pork fat extract (lard)

Also Published As

Publication number Publication date
DE1203909B (de) 1965-10-28
NL302091A (en:Method)
FR3104M (fr) 1965-02-01
CH465139A (de) 1968-11-15
BE641559A (en:Method) 1964-04-16
GB1018647A (en) 1966-01-26

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